8TLM
Structure of a class A GPCR/Fab complex
8TLM の概要
| エントリーDOI | 10.2210/pdb8tlm/pdb |
| EMDBエントリー | 41370 |
| 分子名称 | Fab heavy chain, Fab light chain, C-C chemokine receptor type 8, Green fluorescent protein fusion (3 entities in total) |
| 機能のキーワード | gpcr fab, structural protein |
| 由来する生物種 | Oryctolagus cuniculus (rabbit) 詳細 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 123181.92 |
| 構造登録者 | |
| 主引用文献 | Sun, D.,Sun, Y.,Janezic, E.,Zhou, T.,Johnson, M.,Azumaya, C.,Noreng, S.,Chiu, C.,Seki, A.,Arenzana, T.L.,Nicoludis, J.M.,Shi, Y.,Wang, B.,Ho, H.,Joshi, P.,Tam, C.,Payandeh, J.,Comps-Agrar, L.,Wang, J.,Rutz, S.,Koerber, J.T.,Masureel, M. Structural basis of antibody inhibition and chemokine activation of the human CC chemokine receptor 8. Nat Commun, 14:7940-7940, 2023 Cited by PubMed Abstract: The C-C motif chemokine receptor 8 (CCR8) is a class A G-protein coupled receptor that has emerged as a promising therapeutic target in cancer. Targeting CCR8 with an antibody has appeared to be an attractive therapeutic approach, but the molecular basis for chemokine-mediated activation and antibody-mediated inhibition of CCR8 are not fully elucidated. Here, we obtain an antagonist antibody against human CCR8 and determine structures of CCR8 in complex with either the antibody or the endogenous agonist ligand CCL1. Our studies reveal characteristic antibody features allowing recognition of the CCR8 extracellular loops and CCL1-CCR8 interaction modes that are distinct from other chemokine receptor - ligand pairs. Informed by these structural insights, we demonstrate that CCL1 follows a two-step, two-site binding sequence to CCR8 and that antibody-mediated inhibition of CCL1 signaling can occur by preventing the second binding event. Together, our results provide a detailed structural and mechanistic framework of CCR8 activation and inhibition that expands our molecular understanding of chemokine - receptor interactions and offers insight into the development of therapeutic antibodies targeting chemokine GPCRs. PubMed: 38040762DOI: 10.1038/s41467-023-43601-8 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.9 Å) |
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